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01 1ALCOHOL
02 1CABERGOLINE
03 3CLONIDINE
04 1DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE
05 2IVABRADINE HYDROCHLORIDE
06 4LEVETIRACETAM
07 1LIFITEGRAST
08 1PANTOPRAZOLE SODIUM
09 1TAFLUPROST
10 2TIMOLOL MALEATE
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01 17INGENUS PHARMS LLC
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01 5SOLUTION/DROPS;OPHTHALMIC
02 1SOLUTION;INTRA-ARTERIAL
03 3SYSTEM;TRANSDERMAL
04 1TABLET, DELAYED RELEASE;ORAL
05 7TABLET;ORAL
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01 10.0015%
02 10.1MG/24HR
03 10.2MG/24HR
04 10.3MG/24HR
05 10.5MG
06 11GM
07 1250MG
08 15%
09 1500MG
10 1750MG
11 199% (5ML)
12 1EQ 0.25% BASE
13 1EQ 0.5% BASE
14 1EQ 2% BASE;EQ 0.5% BASE
15 1EQ 40MG BASE
16 1EQ 5MG BASE
17 1EQ 7.5MG BASE
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01 17USA
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Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRA-ARTERIAL
Brand Name : DEHYDRATED ALCOHOL
Dosage Strength : 99% (5ML)
Packaging :
Approval Date : 2025-07-09
Application Number : 219569
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CABERGOLINE
Dosage Strength : 0.5MG
Packaging :
Approval Date : 2018-08-01
Application Number : 204735
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SYSTEM;TRANSDERMAL
Brand Name : CLONIDINE
Dosage Strength : 0.1MG/24HR
Packaging :
Approval Date : 2009-08-18
Application Number : 76157
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SYSTEM;TRANSDERMAL
Brand Name : CLONIDINE
Dosage Strength : 0.2MG/24HR
Packaging :
Approval Date : 2009-08-18
Application Number : 76157
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SYSTEM;TRANSDERMAL
Brand Name : CLONIDINE
Dosage Strength : 0.3MG/24HR
Packaging :
Approval Date : 2009-08-18
Application Number : 76157
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE
Dosage Form : SOLUTION/DROPS;OPHTHALMI...
Brand Name : DORZOLAMIDE HYDROCHLORIDE...
Dosage Strength : EQ 2% BASE;EQ 0.5% BAS...
Packaging :
Approval Date : 2023-05-01
Application Number : 217260
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : IVABRADINE HYDROCHLORIDE
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2021-12-30
Application Number : 214051
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : IVABRADINE HYDROCHLORIDE
Dosage Strength : EQ 7.5MG BASE
Packaging :
Approval Date : 2021-12-30
Application Number : 214051
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : LEVETIRACETAM
Dosage Strength : 250MG
Packaging :
Approval Date : 2009-01-15
Application Number : 79042
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : LEVETIRACETAM
Dosage Strength : 500MG
Packaging :
Approval Date : 2009-01-15
Application Number : 79042
Regulatory Info : RX
Registration Country : USA

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